FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Secret Pro

K Number: K233374 · Decision Dec 14, 2023
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
16
Review Days
73

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Basic Information

Device Name
Secret Pro
K Number
K233374
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ilooda Co,., Ltd.
Date Received
October 2, 2023
Decision Date
December 14, 2023
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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K202043 Secret Duo
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